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Figure 6 | Orphanet Journal of Rare Diseases

Figure 6

From: Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy

Figure 6

Secondary structures prediction of MYH7B. (A) Secondary structures predictions for the MYH7B-890R (left) and MYH7B-890C (right) proteins. The program also performed an accurate prediction of the real-valued relative solvent accessibility. The 890 R to C amino acid substitution changes the beta strands (green arrows) and alpha helix (red lines) structures of the MYH7B protein. All changes are indicated with black arrows. (B) Enlarged area with the region containing the mutation highlighted.

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172